Variant report

Variant	esv3375515
Chromosome Location	chr1:227921854-227924702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:633)
CpG islands
(count:672)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227922943-227923221	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:227922876-227923200	K562	blood:	n/a	n/a
3	ATF2	chr1:227922773-227923310	GM12878	blood:	n/a	n/a
4	ATF2	chr1:227922771-227923204	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:227922752-227923205	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:227922840-227923246	GM12878	blood:	n/a	n/a
7	ATF3	chr1:227922853-227923260	K562	blood:	n/a	n/a
8	ATF3	chr1:227922771-227923314	A549	lung:	n/a	n/a
9	ATF3	chr1:227922794-227923294	A549	lung:	n/a	n/a
10	ATF3	chr1:227922964-227923270	K562	blood:	n/a	n/a
11	BACH1	chr1:227922801-227923199	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:227922879-227923168	GM12878	blood:	n/a	n/a
13	BCL3	chr1:227922700-227923314	A549	lung:	n/a	chr1:227922701-227922710
14	BCL3	chr1:227922711-227923304	A549	lung:	n/a	n/a
15	BCLAF1	chr1:227922726-227923328	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:227922735-227923327	K562	blood:	n/a	n/a
17	BCLAF1	chr1:227922792-227923275	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:227922768-227923324	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:227922792-227923383	K562	blood:	n/a	n/a
20	BHLHE40	chr1:227922815-227923247	HepG2	liver:	n/a	n/a
21	BRCA1	chr1:227922831-227923202	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr1:227922810-227923143	GM12878	blood:	n/a	n/a
23	BRCA1	chr1:227922849-227923213	HepG2	liver:	n/a	n/a
24	BRCA1	chr1:227922876-227923207	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr1:227922855-227923211	K562	blood:	n/a	n/a
26	CBX3	chr1:227922729-227923282	K562	blood:	n/a	n/a
27	CCNT2	chr1:227922642-227923340	K562	blood:	n/a	chr1:227923318-227923327
28	CEBPB	chr1:227922774-227923311	A549	lung:	n/a	n/a
29	CEBPB	chr1:227922858-227923193	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:227922969-227923105	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:227922891-227923179	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPD	chr1:227922725-227923408	HepG2	liver:	n/a	n/a
33	CEBPD	chr1:227922815-227923402	K562	blood:	n/a	n/a
34	CEBPD	chr1:227922801-227923269	HepG2	liver:	n/a	n/a
35	CHD1	chr1:227922681-227923239	GM12878	blood:	n/a	n/a
36	CHD1	chr1:227923500-227923631	GM12878	blood:	n/a	n/a
37	CHD1	chr1:227922881-227923121	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:227922744-227923336	GM12878	blood:	n/a	n/a
39	CHD2	chr1:227922810-227923236	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:227922488-227923312	Hela-S3	cervix:	n/a	chr1:227922680-227922690
41	CHD2	chr1:227922770-227923296	HepG2	liver:	n/a	n/a
42	CHD2	chr1:227922811-227923215	K562	blood:	n/a	n/a
43	CREB1	chr1:227922724-227923457	K562	blood:	n/a	n/a
44	CREB1	chr1:227922836-227923288	A549	lung:	n/a	n/a
45	CREB1	chr1:227922621-227923439	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr1:227922265-227923512	HepG2	liver:	n/a	n/a
47	CREB1	chr1:227922690-227923346	GM12878	blood:	n/a	n/a
48	CREB1	chr1:227922810-227923477	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:227922679-227923311	A549	lung:	n/a	n/a
50	CTCF	chr1:227922920-227923070	GM12865	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227922533-227922583	Hepatocyte	liver:	n/a
2	chr1:227922533-227922583	Hepatocyte	liver:	n/a
3	chr1:227922309-227922359	HIPEpiC	eye:	n/a
4	chr1:227923227-227923277	Caco-2	colon:	n/a
5	chr1:227922863-227922913	H1-hESC	embryonic stem cell:	embryo
6	chr1:227922304-227922354	HL-60	blood:	n/a
7	chr1:227922309-227922359	GM12891	blood:	n/a
8	chr1:227924055-227924105	HCT-116	colon:	n/a
9	chr1:227922863-227922913	MCF-7	breast:	n/a
10	chr1:227922533-227922583	U87	brain:	n/a
11	chr1:227922838-227922888	HCF	heart:	n/a
12	chr1:227922838-227922888	GM06990	blood:	n/a
13	chr1:227924115-227924165	HEEpiC	esophagus:	n/a
14	chr1:227922304-227922354	H1-hESC	embryonic stem cell:	embryo
15	chr1:227922334-227922384	AG04450	lung:	fetal
16	chr1:227924115-227924165	HUVEC	blood vessel:	n/a
17	chr1:227922533-227922583	HNPCEpiC	eye:	n/a
18	chr1:227923938-227923988	HIPEpiC	eye:	n/a
19	chr1:227924115-227924165	NH-A	brain:	n/a
20	chr1:227923227-227923277	HRPEpiC	eye:	n/a
21	chr1:227922512-227922562	HL-60	blood:	n/a
22	chr1:227922533-227922583	PANC-1	pancreas:	n/a
23	chr1:227923227-227923277	LNCaP	prostate:	n/a
24	chr1:227923227-227923277	GM06990	blood:	n/a
25	chr1:227922838-227922888	PANC-1	pancreas:	n/a
26	chr1:227924055-227924105	RPTEC	kidney:	n/a
27	chr1:227924115-227924165	PANC-1	pancreas:	n/a
28	chr1:227924115-227924165	AG04449	skin:	fetal
29	chr1:227923938-227923988	GM12891	blood:	n/a
30	chr1:227922863-227922913	Caco-2	colon:	n/a
31	chr1:227924055-227924105	H1-hESC	embryonic stem cell:	embryo
32	chr1:227922512-227922562	HAEpiC	amniotic membrane:	n/a
33	chr1:227922533-227922583	HEK293	kidney:	embryo
34	chr1:227924055-227924105	GM06990	blood:	n/a
35	chr1:227922334-227922384	GM06990	blood:	n/a
36	chr1:227922533-227922583	HMEC	breast:	n/a
37	chr1:227922533-227922583	GM06990	blood:	n/a
38	chr1:227922304-227922354	HUVEC	blood vessel:	n/a
39	chr1:227924115-227924165	ProgFib	skin:	n/a
40	chr1:227922304-227922354	Hela-S3	cervix:	n/a
41	chr1:227922533-227922583	GM12892	blood:	n/a
42	chr1:227923227-227923277	NHBE	bronchial:	n/a
43	chr1:227922309-227922359	ovcar-3	ovarian:	n/a
44	chr1:227924115-227924165	Hela-S3	cervix:	n/a
45	chr1:227922863-227922913	HCM	heart:	n/a
46	chr1:227924055-227924105	NHDF-neo	bronchial:	n/a
47	chr1:227923227-227923277	HCF	heart:	n/a
48	chr1:227922309-227922359	SK-N-SH_RA	brain:	n/a
49	chr1:227922512-227922562	HCM	heart:	n/a
50	chr1:227924115-227924165	IMR90	lung:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227921956..227924183-chr1:227932541..227935696,3	MCF-7	breast:
2	chr1:227750240..227752795-chr1:227921793..227923560,2	K562	blood:
3	chr1:227921488..227923041-chr1:228269667..228272192,2	MCF-7	breast:
4	chr1:227923000..227925656-chr1:228268639..228271303,2	MCF-7	breast:
5	chr1:227921116..227923050-chr1:228289460..228292114,2	MCF-7	breast:
6	chr1:227922958..227924817-chr1:228133058..228135872,2	MCF-7	breast:
7	chr1:227922748..227923393-chr18:10525883..10526533,2	Hela-S3	cervix:
8	chr1:227916221..227923035-chr1:228131852..228141791,18	MCF-7	breast:
9	chr1:227922541..227923238-chr20:21283483..21284425,2	HCT-116	colon:
10	chr1:227918805..227924684-chr1:227929963..227939883,12	K562	blood:
11	chr1:227754198..227755750-chr1:227920040..227921876,2	K562	blood:

No data

Variant related genes	Relation type
SNAP47	TF binding region
JMJD4	TF binding region
SNAP47	CpG island
JMJD4	CpG island
ENSG00000143816	chromatin interactions
ENSG00000143740	chromatin interactions
ENSG00000181450	chromatin interactions
ENSG00000143761	chromatin interactions
ENSG00000230005	chromatin interactions
ENSG00000088930	chromatin interactions
ENSG00000134265	chromatin interactions
ENSG00000143793	chromatin interactions

Extended variants
information (count: 166 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:166 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13374928	chr1:227921875-227921876	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs138775161	chr1:227921926-227921927	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs537361968	chr1:227921964-227921965	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs186098333	chr1:227921990-227921991	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs111395560	chr1:227922009-227922010	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs150599651	chr1:227922014-227922015	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs141876853	chr1:227922027-227922028	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs574673897	chr1:227922030-227922031	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs541688828	chr1:227922033-227922034	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs563484082	chr1:227922035-227922036	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs568917999	chr1:227922054-227922055	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs563278823	chr1:227922077-227922078	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs56684758	chr1:227922078-227922079	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs570798973	chr1:227922079-227922080	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs530534124	chr1:227922081-227922082	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs375331569	chr1:227922092-227922093	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs368593125	chr1:227922118-227922119	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs551140553	chr1:227922140-227922141	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs565891661	chr1:227922141-227922142	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs13373816	chr1:227922142-227922143	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs371020547	chr1:227922149-227922150	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs528036331	chr1:227922160-227922161	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs546563473	chr1:227922162-227922163	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs146263533	chr1:227922183-227922184	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs375399578	chr1:227922216-227922217	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs530396402	chr1:227922242-227922243	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs4559498	chr1:227922286-227922287	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs368886090	chr1:227922311-227922312	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs373083206	chr1:227922314-227922315	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs570237031	chr1:227922352-227922353	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs376894516	chr1:227922371-227922372	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs199647402	chr1:227922391-227922392	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs201330178	chr1:227922400-227922401	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs572621463	chr1:227922410-227922411	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs34226061	chr1:227922412-227922413	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs200622561	chr1:227922413-227922414	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs199923105	chr1:227922446-227922447	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs141350097	chr1:227922448-227922449	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs151008919	chr1:227922452-227922453	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs138383272	chr1:227922458-227922459	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs371069318	chr1:227922462-227922463	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs373064733	chr1:227922471-227922472	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs376321647	chr1:227922477-227922478	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs148842395	chr1:227922479-227922480	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs200460718	chr1:227922485-227922486	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs373897456	chr1:227922517-227922518	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs368012268	chr1:227922529-227922530	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs183479449	chr1:227922533-227922534	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs202057877	chr1:227922549-227922550	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs386639986	chr1:227922564-227922565	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227917200-227922000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:227918400-227922000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:227918600-227922000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:227918600-227922000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr1:227919000-227922000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:227920400-227922000	Genic enhancers	Right Ventricle	heart
7	chr1:227920600-227922000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
8	chr1:227920800-227922000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:227920800-227922000	Genic enhancers	Gastric	stomach
10	chr1:227921000-227922000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr1:227921200-227922000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:227921200-227922000	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr1:227921200-227922000	Enhancers	Primary T cells fromperipheralblood	blood
14	chr1:227921200-227922000	Enhancers	Brain Angular Gyrus	brain
15	chr1:227921200-227922200	Enhancers	Primary B cells from peripheral blood	blood
16	chr1:227921200-227922200	Weak transcription	Aorta	Aorta
17	chr1:227921400-227922000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:227921400-227922000	Enhancers	Primary B cells from cord blood	blood
19	chr1:227921400-227922000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr1:227921400-227922000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:227921400-227922000	Enhancers	Brain Hippocampus Middle	brain
22	chr1:227921400-227922000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr1:227921400-227922000	Enhancers	Fetal Brain Male	brain
24	chr1:227921400-227922000	Genic enhancers	Left Ventricle	heart
25	chr1:227921400-227922000	Enhancers	Thymus	Thymus
26	chr1:227921400-227922000	Flanking Active TSS	HepG2	liver
27	chr1:227921400-227922000	Flanking Active TSS	HMEC	breast
28	chr1:227921400-227922000	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr1:227921400-227922200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr1:227921400-227922200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr1:227921400-227922600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:227921600-227922000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:227921600-227922000	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr1:227921600-227922000	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr1:227921600-227922000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:227921600-227922000	Enhancers	Brain Anterior Caudate	brain
37	chr1:227921600-227922000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr1:227921600-227922000	Enhancers	Fetal Lung	lung
39	chr1:227921600-227922000	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr1:227921600-227922000	Flanking Active TSS	Hela-S3	cervix
41	chr1:227921600-227922000	Flanking Active TSS	HSMM	muscle
42	chr1:227921600-227922000	Flanking Active TSS	K562	blood
43	chr1:227921600-227922000	Flanking Active TSS	NHDF-Ad	bronchial
44	chr1:227921600-227922200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr1:227921600-227922200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr1:227921600-227922200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr1:227921600-227922200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:227921600-227922200	Enhancers	Esophagus	oesophagus
49	chr1:227921600-227922200	Enhancers	Fetal Heart	heart
50	chr1:227921600-227922200	Enhancers	Lung	lung

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